GLYCOSYLATION DISORDER SYNDROME TYPE 1b: DIAGNOSTICS AND TREATMENT
The article highlights the medical case of a rare hereditary disease — glycosylation disorder syndrome type 1b, unique for our country. This syndrome is referred to the heterogeneous group of the congenital diseases characterized by the disorder of glycoprotein synthesis as a result of the defects N...
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| Hauptverfasser: | , , , , , , , |
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| Format: | Artigo |
| Sprache: | Russo |
| Veröffentlicht: |
Union of pediatricians of Russia
2008-09-01
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| Schriftenreihe: | Педиатрическая фармакология |
| Online-Zugang: | https://www.pedpharma.ru/jour/article/view/765 |
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